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Distinct Gene Expression and Epigenetic Signatures in Hepatocyte-like Cells Produced by Different Strategies from the Same Donor

机译:同一供体不同策略产生的肝细胞样细胞中不同的基因表达和表观遗传特征

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Summary Hepatocyte-like cells (HLCs) can be generated through directed differentiation or transdifferentiation. Employing two strategies, we generated induced pluripotent stem cell (iPSC)-HLCs and hiHeps from the same donor cell line. Both types of HLCs clustered distinctly from each other during gene expression profiling. In particular, differences existed in gene expression for phase II drug metabolism and lipid accumulation, underpinned by H3K27 acetylation status in iPSC-HLCs and hiHeps. While distinct phenotypes were achieved in?vitro , both types of HLCs demonstrated similar phenotypes following transplantation into Fah-deficient mice. In conclusion, functional HLCs can be obtained from the same donor using two strategies. Global gene expression defined the differences between those populations in?vitro . Importantly, both HLCs displayed partial but markedly improved hepatic function following transplantation in?vivo , demonstrating plasticity and the potential for cell-based modeling in the dish and cell-based therapy in the future.
机译:总结肝细胞样细胞(HLC)可以通过定向分化或转分化产生。采用两种策略,我们从同一供体细胞系中产生了诱导性多能干细胞(iPSC)-HLC和hiHeps。在基因表达谱分析中,两种类型的HLC彼此明显地聚集在一起。特别是,在iPSC-HLC和hiHeps中,H3K27乙酰化状态支持了II期药物代谢和脂质积聚的基因表达差异。虽然体外获得了不同的表型,但两种类型的HLC在移植到Fah缺陷型小鼠中后均表现出相似的表型。总之,可以使用两种策略从同一供体中获得功能性HLC。全球基因表达定义了这些体外种群之间的差异。重要的是,两个HLCs在体内移植后均显示出部分但明显改善的肝功能,这表明可塑性以及将来在培养皿和基于细胞的治疗中基于细胞的建模的潜力。

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